Advanced search
Publication Cover
Audiological Medicine Volume 1, 2003 - Issue 1
Journal homepage
63
Views
21
CrossRef citations to date
0
Altmetric
Research Article

Audiological Manifestations and Features of Connexin 26 Deafness

GLENN E GREEN Department of Surgery University of Arizona Tucson AZ USACorrespondence[email protected]
,
ROBERT F MUELLER Department of Clinical Genetics St James's Hospital Leeds UK
,
EDWARD S COHN Center for Ear, Hearing and Balance Disorders Boys Town National Research Hospital Omaha NE USA
,
KAREN B AVRAHAM Department of Human Genetics and Molecular Medicine Sackler School of Medicine Tel Aviv University Tel Aviv Israel
,
MOIEN KANAAN Molecular Genetics, Life Science Department Bethlehem University POB 9 Palestinian Authority Israel
&
RICHARD JH SMITH Department of Otolaryngology and Interdepartmental Genetics Program University of Iowa Iowa City IA USA
Pages 5-11 | Published online: 11 Jul 2009

Citations (21)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (2)

Anna Berto, Daniela Pellati, Alessandro Castiglione, Micol Busi, Patrizia Trevisi, Francesca Gualandi, Alessandra Ferlini & Alessandro Martini. (2009) Audiological profiles and gjb2, gjb6 mutations: A retrospective study on genetic and clinical data from 2003 to 2008. Audiological Medicine 7:2, pages 93-105.
Read now
Silvano Prosser & Alessandro Martini. (2005) Editorial. Audiological Medicine 3:3, pages 147-153.
Read now

Articles from other publishers (19)

Kari L. Green, Donald L. Swiderski, Diane M. Prieskorn, Susan J. DeRemer, Lisa A. Beyer, Josef M. Miller, Glenn E. Green & Yehoash Raphael. (2016) ACEMg Diet Supplement Modifies Progression of Hereditary Deafness. Scientific Reports 6:1.
Crossref
A. Eliot Shearer, Robert W. Eppsteiner & Richard J. H. Smith. 2016. Molecular Pathology in Clinical Practice. Molecular Pathology in Clinical Practice 197 201 .
N. L. Kunel’skaya, E. V. Garov, E. E. Zagorskaya, A. S. Sheremet, E. V. Baibakova & Ya. Yu. Kudeeva. (2015) The application of ultrasound for diagnostics of middle ear pathologies. Vestnik otorinolaringologii 80:2, pages 12.
Crossref
Glenn Green & Yehoash Raphael. 2015. Free Radicals in ENT Pathology. Free Radicals in ENT Pathology 377 391 .
Aaron Thatcher, Colleen Le Prell, Josef Miller & Glenn Green. (2014) ACEMg supplementation ameliorates progressive Connexin 26 hearing loss in a child. International Journal of Pediatric Otorhinolaryngology 78:3, pages 564-566.
Crossref
Ö Tarkan, P Sari, O Demirhan, M Kiroğlu, Ü Tuncer, Ö Sürmelioğlu, S Özdemir, M B Yilmaz & K Kara. (2012) Connexin 26 and 30 mutations in paediatric patients with congenital, non-syndromic hearing loss treated with cochlear implantation in Mediterranean Turkey. The Journal of Laryngology & Otology 127:1, pages 33-37.
Crossref
Simon Angeli, Xi Lin & Xue Zhong Liu. (2012) Genetics of Hearing and Deafness. The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology 295:11, pages 1812-1829.
Crossref
Diana P. Popova, Radka Kaneva, Sonya Varbanova & Todor M. Popov. (2011) Prevalence of GBJ2 mutations in patients with severe to profound congenital nonsyndromic sensorineural hearing loss in Bulgarian population. European Archives of Oto-Rhino-Laryngology 269:6, pages 1589-1592.
Crossref
Jordan B. Hochman, Tracy L. Stockley, D. Shipp, Vincent Y. W. Lin, Joseph M. Chen & Julian M. Nedzelski. (2010) Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) Mutations in a Population of Adult Cochlear Implant Candidates. Otology & Neurotology 31:6, pages 919-922.
Crossref
S. G. Zhuravskiy, A. A. Kurus, A. E. Taraskina & S. A. Ivanov. (2009) Ultrastructure of the Hair in Genetic Prelingual Deafness Associated with the 35delG Mutation in the Connexin 26 Gene (GJB2). Bulletin of Experimental Biology and Medicine 148:1, pages 79-81.
Crossref
Amit Kochhar, Simon I. Angeli, Sandeep P. Dave & Xue Z. Liu. (2009) Imaging correlation of children with DFNB1 vs non‐DFNB1 hearing loss. Otolaryngology–Head and Neck Surgery 140:5, pages 665-669.
Crossref
Richard J.H. Smith & Guy Van Camp. 2009. Molecular Pathology in Clinical Practice: Genetics. Molecular Pathology in Clinical Practice: Genetics 123 131 .
Y. Bajaj, T. Sirimanna, D.M. Albert, P. Qadir, L. Jenkins & M. Bitner-Glindzicz. (2008) Spectrum of GJB2 mutations causing deafness in the British Bangladeshi population . Clinical Otolaryngology 33:4, pages 313-318.
Crossref
Yuelin Li, Annie G. Steinberg, Lisa Bain, Dinah Yaeger, Ari Bieler, Rachel Ewing, Girija Kaimal & Ian Krantz. (2007) Assessing parental attitudes toward genetic testing for childhood hearing loss: Before and after genetic consultation. American Journal of Medical Genetics Part A 143A:14, pages 1546-1553.
Crossref
Richard J. H. Smith & Guy Van Camp. 2007. Molecular Pathology in Clinical Practice. Molecular Pathology in Clinical Practice 125 133 .
Evan J. Propst, Susan Blaser, Tracy L. Stockley, Robert V. Harrison, Karen A. Gordon & Blake C. Papsin. (2006) Temporal Bone Imaging in GJB2 Deafness. The Laryngoscope 116:12, pages 2178-2186.
Crossref
Attila Torkos, Magnus Teschner, Peter Erfurt, Gerrit Paasche, Thomas Lenarz & Timo Stöver. (2006) The use of buccal smears for a non-invasive screening of the 35delG mutation of the Connexin-26 gene in hearing impaired young children. International Journal of Pediatric Otorhinolaryngology 70:6, pages 965-971.
Crossref
Hela Azaiez, G. Parker Chamberlin, Stephanie M. Fischer, Chelsea L. Welp, Sai D. Prasad, R. Thomas Taggart, Ignacio del Castillo, Guy Van Camp & Richard J. H. Smith. (2004) GJB2: The spectrum of deafness-causing allele variants and their phenotype. Human Mutation 24:4, pages 305-311.
Crossref
Richard J.H. Smith. (2004) Clinical application of genetic testing for deafness. American Journal of Medical Genetics Part A 130A:1, pages 8-12.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.